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Allogenic stem cell transplantation for bone marrow failure syndrome, experience from the Bone Marrow Transplant Unit at the Clínica de Marly.

Trasplante alogénico de progenitores hematopoyéticos para síndromes de falla medular, experiencia de la Unidad de Trasplante de Médula Ósea de la Clínica de Marly.




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Original articles

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Allogenic stem cell transplantation for bone marrow failure syndrome, experience from the Bone Marrow Transplant Unit at the Clínica de Marly.
Rev. colomb. hematol. oncol. [Internet]. 2012 Apr. 1 [cited 2024 Dec. 22];1(1):44-51. Disponible en: https://doi.org/10.51643/22562915.287

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PlumX
Virginia Abello
    Licet Villamizar
      Enrique Pedraza
        Herman Esguerra
          Carmen Rosales

            Virginia Abello,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).  Fundación Universitaria de Ciencias de la Salud, Hospital de San José (Bogotá, Colombia)


            Licet Villamizar,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).  Fundación Universitaria de Ciencias de la Salud, Hospital de San José (Bogotá, Colombia)


            Enrique Pedraza,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).


            Herman Esguerra,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).


            Carmen Rosales,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).


            Adriana Linares,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).


            Manuel Rosales,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).


            Javier Figueroa,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).


            William Mantilla,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).


            Claudia Casas,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).  Fundación Universitaria de Ciencias de la Salud, Hospital de San José (Bogotá, Colombia)


            Nathalia Villaroya,

            Unidad de Trasplante de Médula Ósea, Clínica de Marly (Bogotá, Colombia).


            Background: Allogeneic hematopoietic stem cell transplantation (allo-SCT) is considered as the treatment of choice for newly diagnosed patients with bone marrow failure syndromes (BMFS) younger than 40 years, and for older patients that have failed immunosuppressive therapy. Methods: This is a retrospective study of BMFS pediatric and adult patients receiving allo-SCT at a single institution from Bogota, Colombia. The primary outcome was five-year overall survival (OS), determined by the Kaplan-Meier method. Log-rank test was used to determine the impact of various factors over OS. In-hospital stay, grade II-IV acute graft versus host disease (aGVHD) and secondary graft failure were explored. Results: Between January 1993 and August 2011, 74 transplants were performed in 70 patients. 70 grafts were obtained from HLA identical siblings, 3 from unrelated umbilical cord blood and 1 from a haploidentical sibling, were obtained from HLA identical siblings, 3 from unrelated CBU and 1 from a haploidentical sibling. Conditioning regimens used were: RIC Cy-Flu-ATG (22), Cy-ATG (33) and Cy (12). 4 patients were conditioned with alemtuzumab containing regimens and 3 with other. Before 2004 most patients received Cs and MTX as GVHD prophylaxis, after 2004 Cs and MMF was used in the majority. Two patients died during the progenitors infusion. Engraftment for 68 evaluable patients at first allo-SCT ocurred at an average of 11.5 days, similarly between conditioning regimens. 10 patients (14%) had secondary graft failure of whom five died at a mean of 178 days after the allo-SCT. Five patients remain alive, two are transfusion-dependent and three succeeded a second allo-SCT. aGVHD occurred in 30% of patients of whom 46.7% died due to related complications; aGVHD was more frequent with ATG non-containing regimens. For a median follow-up of 18.4 months (range: 4.3- 45.3) OS was 69.1% and varied according to conditioning combination (p = 0.0008). There was no significant difference for OS related to age (p = 0.67). A greater but not significant OS was observed for allo-SCT performed after than before 2004 (p = 0.38). Conclusions: This experience showed that allo-SCT is a fundamental therapeutic option for patients with BMFS treated with allo-SCT, offering a better OS regardless the age and year of performance, suggesting an advantage for RIC over other conditioning regimens.


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            1. Young NS, Maciejewski J. The pathophysiology of acquired aplastic anemia. N Engl J Med. 1997;336(19):1365-72.
            2. Marsh JC, Ball SE, Cavenagh J, Darbyshire P, Dokal I, GordonSmith EC, et al. Guidelines for the diagnosis and management of aplastic anaemia. Br J Haematol. 2009;147(1):43-70.
            3. Sanders JE, Storb R, Anasetti C, Deeg HJ, Doney K, Sullivan KM, et al. Marrow transplant experience for children with severe aplastic anemia. Am J Pediatr Hematol Oncol. 1994;16(1):43-9.
            4. Medeiros LA, Pasquini R. Anemia aplásica adquirida e anemia de Fanconi: diretrizes brasileiras em transplante de células-tronco hematopoéticas. Rev Bras Hematol Hemoter. 2010;32(supl 1):40-5.
            5. Deeg HJ, Leisenring W, Storb R, Nims J, Flowers ME, Witherspoon RP, et al. Long-term outcome after marrow transplantation for severe aplastic anemia. Blood. 1998;91(10):3637-45.
            6. Gluckman E, Socie G, Devergie A, Bourdeau-Esperou H, Traineau R, Cosset JM. Bone marrow transplantation in 107 pa tients with severe aplastic anemia using cyclophosphamide and thoraco-abdominal irradiation for conditioning: long-term follow-up. Blood. 1991;78(9):2451-5.
            7. Bacigalupo A, Brand R, Oneto R, Bruno B, Socie G, Passweg J, et al. Treatment of acquired severe aplastic anemia: bone marrow transplantation compared with immunosuppressive therapy--The European Group for Blood and Marrow Transplantation experience. Semin Hematol. 2000;37(1):69-80.
            8. Arranz R, Conde E, Rodriguez-Salvanes F, Pajuelo FJ, Cabrera R, Sanz MA, et al. CsA-based post-graft immunosuppression: the main factor for improving outcome of allografted patients with acquired aplastic anemia. A retrospective survey by the Spanish Group of Hematopoietic Transplantation. Bone Marrow Transplant. 2002;29(3):205-11.
            9. Ades L, Mary JY, Robin M, Ferry C, Porcher R, Esperou H, et al. Long-term outcome after bone marrow transplantation for severe aplastic anemia. Blood. 2004;103(7):2490-7.
            10. Kim I, Yoon SS, Park S, Kim BK, Kim NK. The treatment of severe aplastic anemia: outcomes of bone marrow transplantation and immunosuppressive therapy in a single institution of Korea. J Korean Med Sci. 2003;18(3):365-71.
            11. Storb R, Blume KG, O’Donnell MR, Chauncey T, Forman SJ, Deeg HJ, et al. Cyclophosphamide and antithymocyte globulin to condition patients with aplastic anemia for allogeneic marrow transplantations: the experience in four centers. Biol Blood Marrow Transplant. 2001;7(1):39-44.
            12. Sangiolo D, Storb R, Deeg HJ, Flowers MED, Martin PJ, Sandmaier BM, et al. Outcome of allogeneic hematopoietic cell transplantation from HLA-identical siblings for severe aplastic anemia in patients over 40 years of age. Biol Blood Marrow Transplant. 2010;16(10):1411-8.
            13. Maury S, Bacigalupo A, Anderlini P, Aljurf M, Marsh J, Socie G, et al. Improved outcome of patients older than 30 years receiving HLA-identical sibling hematopoietic stem cell transplantation for severe acquired aplastic anemia using fludarabine-based conditioning: a comparison with conventional conditioning regimen. Haematologica. 2009;94(9):1312-5.
            14. Glucksberg H, Storb R, Fefer A, Buckner CD, Neiman PE, Clift RA, et al. Clinical manifestations of graft-versus-host disease in human recipients of marrow from HL-A-matched sibling donors. Transplantation. 1974;18(4):295-304.
            15. Champlin RE, Horowitz MM, van Bekkum DW, Camitta BM, Elfenbein GE, Gale RP, et al. Graft failure following bone marrow transplantation for severe aplastic anemia: risk factors and treatment results. Blood. 1989;73(2):606-13.
            16. Camitta BM, Storb R, Thomas ED. Aplastic anemia (first of two parts): pathogenesis, diagnosis, treatment, and prognosis. N Engl J Med. 1982;306(11):645-52.
            17. Locasciulli A, Oneto R, Bacigalupo A, Socié G, Korthof E, Bekassy A, et al. Outcome of patients with acquired aplastic anemia given first line bone marrow transplantation or immunosuppressive treatment in the last decade: a report from the European Group for Blood and Marrow Transplantation. Haematologica. 2007;92(1):11-8.
            18. Barriga CF, Wietstruck PA, Becker KA, Zúñiga CP, de Besa CP, Álvarez ZM, et al. Tratamiento de anemia aplásica severa adquirida en pacientes pediátricos con inmunosupresión y trasplante alogénico de precursores hematopoyéticos. [Treatment of acquired severe aplastic anemia in pediatric patients with immunosupression and allogeneic stem cell hematopoyetic transplant]. Rev Med Chil. 2007;135(11):1421-8.
            19. Passweg JR, Socie G, Hinterberger W, Bacigalupo A, Biggs JC, Camitta BM, et al. Bone marrow transplantation for severe aplastic anemia: has outcome improved? Blood. 1997;90(2):858-64.
            20. Chu R, Brazauskas R, Kan F, Bashey A, Bredeson C, Camitta B, et al. Comparison of outcomes after transplantation of GCSF–stimulated bone marrow grafts versus bone marrow or peripheral blood grafts from HLA-matched sibling donors for patients with severe aplastic anemia. Biol Blood Marrow Transplant. 2011;17(7):1018-24.
            21. Ghavamzadeh A, Alimoghaddam K, Hamidieh AA, Jalili M, Bahar B, Iravani M, et al. Peripheral blood stem cell transplantation versus bone marrow transplantation in severe aplastic anemia. Biol Blood Marrow Transplant. 2011;17(2):S291.
            22. George B, Mathews V, Viswabandya A, Kavitha ML, Srivastava A, Chandy M. Fludarabine and cyclophosphamide based reduced intensity conditioning (RIC) regimens reduce rejection and improve outcome in Indian patients undergoing allogeneic stem cell transplantation for severe aplastic anemia. Bone Marrow Transplant. 2007;40(1):13-8.
            23. Storb R, Etzioni R, Anasetti C, Appelbaum F, Buckner CD, Bensinger W, et al. Cyclophosphamide combined with antithymocyte globulin in preparation for allogeneic marrow transplants in patients with aplastic anemia. Blood. 1994;84(3):941-9.
            24. Champlin RE, Perez WS, Passweg JR, Klein JP, Camitta BM, Gluckman E, et al. Bone marrow transplantation for severe aplastic anemia: a randomized controlled study of conditioning regimens. Blood. 2007;109(10):4582-5.
            25. Champlin RE, Perez WS, Passweg J, Klein JP, Camitta BM, Gluckman E, et al. Addition of antithymocyte globulin (ATG) to cyclophosphamide (Cy) for HLA-identical sibling allogeneic bone marrow transplantation (BMT) for severe aplastic anemia (SAA): results of a randomized controlled trial. Blood. 2003;102(11):80a.
            26. Kapelushnik J, Or R, Slavin S, Nagler A. A fludarabine-based protocol for bone marrow transplantation in Fanconi’s anemia. Bone Marrow Transplant. 1997;20(12):1109-10.
            27. Bacigalupo A, Locatelli F, Lanino E, Marsh J, Socie G, Maury S, et al. Fludarabine, cyclophosphamide and anti-thymocyte globulin for alternative donor transplants in acquired severe aplastic anemia: a report from the EBMT-SAA Working Party. Bone Marrow Transplant. 2005;36(11):947-50.
            28. Kumar R, Prem S, Mahapatra M, Seth T, Chowdhary DR, Mishra P, et al. Fludarabine, cyclophosphamide and horse antithymocyte globulin conditioning regimen for allogeneic peripheral blood stem cell transplantation performed in non-HEPA filter rooms for multiply transfused patients with severe aplastic anemia. Bone Marrow Transplant. 2006;37(8):745-9.
            29. Locatelli F, Zecca M, Pession A, Morreale G, Longoni D, Di Bartolomeo P, et al. The outcome of children with Fanconi anemia given hematopoietic stem cell transplantation and the influence of fludarabine in the conditioning regimen: a report from the Italian pediatric group. Haematologica. 2007;92(10):1381-8.
            30. Ringden O, Remberger M, Svenberg P, Svahn BM, Dahllof G, Gustafsson B, et al. Fludarabine-based disease-specific conditioning or conventional myeloablative conditioning in hematopoietic stem cell transplantation for treatment of non-malignant diseases. Bone Marrow Transplant. 2007;39(7):383-8.
            31. George B, Mathews V, Viswabandya A, Kavitha ML, Srivastava A, Chandy M. Fludarabine based reduced intensity conditioning regimens in children undergoing allogeneic stem cell transplantation for severe aplastic anemia. Pediatr Transplant. 2008;12(1):14-9.
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